稳健性(进化)
硅
阳极
聚合物
材料科学
合理设计
戊二醛
复合材料
粘附
电化学
纳米技术
化学工程
化学
电极
光电子学
有机化学
物理化学
工程类
基因
生物化学
作者
Pengfei Cao,Guang Yang,Bingrui Li,Yiman Zhang,Sheng Zhao,Shuo Zhang,Andrew Erwin,Zhengcheng Zhang,Alexei P. Sokolov,Jagjit Nanda,Tomonori Saito
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2019-04-22
卷期号:4 (5): 1171-1180
被引量:131
标识
DOI:10.1021/acsenergylett.9b00815
摘要
Although several principles have been recognized to fabricate a nominal "better" binder, there continues to be a lack of a rational design and synthesis approach that would meet the robust criteria required for silicon (Si) anodes. Herein, we report a synthetic polymer binder, i.e., catechol-functionalized chitosan cross-linked by glutaraldehyde (CS-CG+GA), that serves dual functionalities: (a) wetness-resistant adhesion capability via catechol grafting and (b) mechanical robustness via in situ formation of a three-dimensional (3D) network. A SiNP-based anode with a designed functional polymer network (CS-CG10%+6%GA) exhibits a capacity retention of 91.5% after 100 cycles (2144 ± 14 mAh/g). Properties that are traditionally considered to be advantageous, including stronger adhesion strength and higher mechanical robustness, do not always improve the binder performance. A clear relationship between these properties and ultimate electrochemical performance is established by assessing the rheological behavior, mechanical property, adhesion force, peel stress, morphology evolution, and semiquantitative evaluation. This study provides a clear path for the rational design of high-performance functional polymer binders for not only Si-based electrodes but also other types of alloy and conversion-based electrodes.
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